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CORDIS · PREVALUNG EU

Biomarkers affecting the transition from cardiovascular disease to lung cancer: towards stratified interception.

Code
PREVALUNG EU
Programme
HORIZON
Call
HORIZON-HLTH-2022-STAYHLTH-02-01
Status
SIGNED
Period
2022-12-01 – 2027-11-30
Total cost (whole consortium)7 166 124 €
EU contribution (whole consortium)7 016 124 €
EU contribution to Bulgarian participants450 625 €

Official data · CORDIS · synced 2026-10-17 10:16 · official record

Participants

OrganisationsRoleCountryGrant
INSTITUT GUSTAVE ROUSSYcoordinatorFR2 444 708 €
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALEparticipantFR796 855 €
ERASMUS UNIVERSITAIR MEDISCH CENTRUM ROTTERDAMparticipantNL726 375 €
UNIVERSITA DEGLI STUDI DI TORINOparticipantIT600 625 €
МЕДИЦИНСКИ УНИВЕРСИТЕТ-ВАРНА "ПРОФ. Д-Р ПАРАСКЕВ ИВ.СТОЯНОВ"participantBG450 625 €
OLINK PROTEOMICS ABparticipantSE427 452 €
BIO-ME ASparticipantNO393 849 €
CENTRE HOSPITALIER REGIONAL DE MARSEILLE ASSISTANCE PUBLIQUE-HOPITAUX MARSEILLEparticipantFR377 494 €
FONDATION HOPITAL SAINT JOSEPHparticipantFR364 610 €
KATHOLIEKE UNIVERSITEIT LEUVENparticipantBE328 531 €
PATIENTS EN RESEAUparticipantFR105 000 €
GUSTAVE ROUSSY TRANSFERTthird partyFR0 €
UNIVERSITY COLLEGE LONDONassociated partnerUK

Description

Cardiovascular disease (CVD) and lung cancer (LC) are leading causes of deaths and intertwined chronic inflammatory processes associated with metabolism reprogramming, clonal hematopoiesis of indeterminate potential (CHIP), intestinal dysbiosis, and maladaptive immunity. CVD prone-tobacco users exhibit a 1-2% yearly incidence of LC. Low dose computed tomography screening programs reduce LC mortality by 20%. Beyond epidemiological scores, risk identification, early cancer detection and interception are mostly based on cell autonomous approaches. Understanding pathophysiological failures linking CVD to LC would allow to take steps for prevention. Based on metabolo-metageno-proteo-immuno-gen-omics, our PREVALUNG prospective study conducted in CVD tobacco consumers allowed to unveil four drivers of early carcinogenesis leading to actionable biomarkers that can be harnessed to pioneer personalized interceptive measures. Four main objectives will be harnessed by 7 academic partners (transdisciplinarity and trialists in interception), 3 diagnostic Biotech Cies and one nutrition Foundation. First, refine and validate in retro- and pro-spective cohorts (>60.000), the 4 classifiers relying on the 4 inflammatory drivers (autophagy/innate immunity/intestinal barrier defects and CHIP) to implement patient stratification. Second, develop and validate robust friendly-user tools monitoring such biomarkers for routine risk assessment. Third, demonstrate the actionability of these biomarkers through a biologically-informed multi-arm randomised trial testing measures targeting each of the 4 main drivers of inflammation using food supplements or pharmacological agents (metformin, anti-NKG2A/PDL-1 Abs, IL-1 inhibitor, probiotics respectively) in addition to diet and life-style changes to return to homeostasis. Fourth, to adapt a secured interface between patients and clinical researchers using these new tools to the longitudinal monitoring of the interceptive measures.

Official data · CORDIS · synced 2026-10-17 10:16 · official record · Licence: © European Union, CC BY 4.0 (Commission reuse policy).